Lee K M, Hayes J J
Department of Biochemistry and Biophysics, University of Rochester Medical Center, Rochester, New York 14642, USA.
Biochemistry. 1998 Jun 16;37(24):8622-8. doi: 10.1021/bi980499y.
We have employed a site-directed photochemical cross-linking procedure to precisely map interactions between nucleosomal DNA and the C-terminal tail of core histone H2A. We find that this tail has the potential to contact multiple sites within the nucleosome and that these contacts are dependent upon the configuration of the complex. This tail contacts DNA near the dyad axis within nucleosome core particles but rearranges to a site near the edge of the nucleosomal DNA when linker DNA is present. Moreover, in the presence of linker histone H1 the contacts near the edge of the nucleosome but not at the dyad are further rearranged. In addition, we present further evidence for the suggestion that the binding of linker histone causes a subtle but global change in core histone-DNA interactions within the nucleosome [Usachenko, S. I., Gavin, I. M., and Bavykin, S. G. (1996) J. Biol. Chem. 271, 3831-3836].
我们采用了一种定点光化学交联程序,以精确绘制核小体DNA与核心组蛋白H2A的C末端尾巴之间的相互作用。我们发现,这条尾巴有可能与核小体内的多个位点接触,并且这些接触取决于复合物的构型。这条尾巴在核小体核心颗粒内靠近二分体轴的位置与DNA接触,但当存在连接DNA时,它会重新排列到核小体DNA边缘附近的一个位点。此外,在存在连接组蛋白H1的情况下,核小体边缘附近而非二分体处的接触会进一步重新排列。此外,我们为连接组蛋白的结合会导致核小体内核心组蛋白-DNA相互作用发生细微但全局性变化的观点提供了进一步的证据[乌萨琴科,S. I.,加文,I. M.,和巴夫金,S. G.(1996年)《生物化学杂志》271,3831 - 3836]。